Alladin Diagnostic, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Alladin Diagnostic, Inc. makes
Alladin Diagnostic, Inc. manufactures diagnostic reagents for laboratory testing, including Leucine Aminopeptidase and Glucose-6-Phosphate Dehydrogenase reagents. These products are designed for use in biochemical assays to measure enzyme activity in clinical samples.
The company’s portfolio includes Class I and Class II devices, with some products authorised via the FDA’s 510(k) pathway. These reagents are listed under U.S. regulatory requirements and are intended for in vitro diagnostic use.
Catalogue
Leucine Aminopeptidase Reagent Ref K844965
Regimes: 510(k) Registry: 510(k)Glucose-6-Phosphate Dehydrogenase Ref K823900
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alladin Diagnostic, Inc. have in the registry?
The registry currently lists 2 devices for Alladin Diagnostic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alladin Diagnostic, Inc.'s devices?
Among its 2 most recently registered devices, Alladin Diagnostic, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Alladin Diagnostic, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Alladin Diagnostic, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alladin Diagnostic, Inc. in the registry?
The most recently registered devices listed for Alladin Diagnostic, Inc. include LEUCINE AMINOPEPTIDASE REAGENT and GLUCOSE-6-PHOSPHATE DEHYDROGENASE.